190 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SURGITRON 4.0 DUAL RF S5-IEC
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ArgenZ ST 98x18 ML C3
FDA UDI
ARGEN CORPORATION, THE·D818123366·Dental porcelain/ceramic restoration kit
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776299217·Minnesota Retractor 5.5", 23mm width, Ebonized
Paxeon Logical
FDA UDI
PAXEON RECONSTRUCTION LLC·08177570201334·Logical G-Series Shell – 3 Holes Size 66-E
Logical G-Series
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215000943·
Logical G-Series Acetabular Shell
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215052195·
OrthoMedFlex
FDA UDI
ORTHOMEDFLEX LLC·M7161111233660·66mm Acetabular Cup (3-hole)
DATEX-OHMEDA 7900 VENTILATOR ENHANCEMENTS
FDA 510(k)
FDA Class 2
·Anesthesiology
RT600
FDA 510(k)
FDA Class 2
·Neurology
VENTO Cup
FDA UDI
AMPLITUDE SAS·03701089514125·
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2013
VERSACARE BED
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·August 20, 2008
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC·Product code GJS·June 10, 2011
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·March 31, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026